Associated Papers
Expanding the Genetic and Clinical Spectrum of Hereditary Angioedema with Normal C1 Inhibitor: Novel Variants and Treatment Insights.
Gao H et al.
Journal of Clinical Immunology, 2025
Novel SERPING1 gene mutations and clinical experience of type 1 hereditary angioedema from North India.
Jindal AK et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology, 2021
A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1.
Johnsrud I et al.
Plos One, 2015
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